基本信息
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职业迁徙
个人简介
Research Interests:
The overall goal of my research program is to understand the molecular mechanisms and cellular functions of specific oncogenes, tumor suppressor genes, miRNAs/target genes, and their associated pathways/genetic networks, in the regulation of the properties of cancer/leukemic stem cells, signal transduction events, metabolism/mitochondria vulnerabilities, immune responses and initiation and progression of human leukemia and drug resistance. The ultimate objective is to identify and characterize key druggable molecules and pathways, using our well-established in vitro and patient-derived xenotransplantation (PDX) models, which will lead to new, rationally designed, more effective, and less toxic, personalized anti-cancer therapies. In particular, we are extremely interested in developing mechanism-based combination therapeutic strategies that can directly target drug-insensitive leukemic stem cells and mutated drug-resistant cells, to improve outcomes in leukemia patients, especially those destined to develop drug resistance. In collaboration with pharmaceutical companies, we have also been testing new therapeutic agents/inhibitors and combination treatment strategies that can effectively eradicate drug-resistant chronic myeloid leukemia (CML) and acute myeloid leukemia (AML) stem/progenitor cells, by exploring novel oncolytic virotherapy, immunotherapy and nonviral gene therapy. These studies have led to several FDA-approved drugs for the treatment of leukemia patients.
The overall goal of my research program is to understand the molecular mechanisms and cellular functions of specific oncogenes, tumor suppressor genes, miRNAs/target genes, and their associated pathways/genetic networks, in the regulation of the properties of cancer/leukemic stem cells, signal transduction events, metabolism/mitochondria vulnerabilities, immune responses and initiation and progression of human leukemia and drug resistance. The ultimate objective is to identify and characterize key druggable molecules and pathways, using our well-established in vitro and patient-derived xenotransplantation (PDX) models, which will lead to new, rationally designed, more effective, and less toxic, personalized anti-cancer therapies. In particular, we are extremely interested in developing mechanism-based combination therapeutic strategies that can directly target drug-insensitive leukemic stem cells and mutated drug-resistant cells, to improve outcomes in leukemia patients, especially those destined to develop drug resistance. In collaboration with pharmaceutical companies, we have also been testing new therapeutic agents/inhibitors and combination treatment strategies that can effectively eradicate drug-resistant chronic myeloid leukemia (CML) and acute myeloid leukemia (AML) stem/progenitor cells, by exploring novel oncolytic virotherapy, immunotherapy and nonviral gene therapy. These studies have led to several FDA-approved drugs for the treatment of leukemia patients.
研究兴趣
论文共 218 篇作者统计合作学者相似作者
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Xiuwei Yan, Xin Gao,Jiawei Dong,Fang Wang,Xiaoyan Jiang,Xueyan Hu,Jiheng Zhang, Nan Wang, Lei Xu,Zhihui Liu,Shaoshan Hu,Hongtao Zhao
Biochemical Geneticspp.1-23, (2024)
Aysha Ansari,Cezary Kucharski,Mahsa Mohseni, Daniel N. M. Sundaram,Joseph M. Brandwein,Xiaoyan Jiang,Hasan Uludag
JOURNAL OF CLINICAL ONCOLOGYno. 16 (2024)
JOURNAL OF CONTROLLED RELEASE (2024): 821-836
Aysha S. Ansari,Cezary Kucharski,Remant KC, Daniel Nisakar, Ramea Rahim,Xiaoyan Jiang,Joseph Brandwein,Hasan Uludağ
Acta Biomaterialia (2024)
ACS PHARMACOLOGY & TRANSLATIONAL SCIENCEno. 9 (2024): 2840-2855
Bloodno. Supplement 1 (2023): 4547-4547
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作者统计
#Papers: 219
#Citation: 4749
H-Index: 37
G-Index: 67
Sociability: 6
Diversity: 0
Activity: 1
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